Lipotox is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Bioactive Nutritional, Inc.. The primary component is Squalene; Cholesterol; Estradiol; Progesterone; Aspartame; Benzalkonium Chloride; Formaldehyde; Methylene Chloride; Methylparaben; Propylparaben; Sodium Benzoate; Anhydrous Trisodium Citrate; Titanium Dioxide; Zinc Oxide; Arsenic Trioxide; Lycopodium Clavatum Spore; Strychnos Nux-vomica Seed; Phosphoric Acid; Phosphorus; Acetic Acid; Corticotropin; Benzoic Acid; Benzyl Alcohol; Boric Acid; Chlorine; Cortisone Acetate; Eugenol; Estrone; Isopropyl Alcohol; Lactic Acid, Dl-; Petrolatum; Phenylbutazone; Lead; Potassium Sorbate; Resorcinol; Salicylic Acid; Sorbitol; Stearyl Alcohol; Xylitol.
Product ID | 43857-0384_27a0c113-2c72-488b-98e8-bf8b20ed47b7 |
NDC | 43857-0384 |
Product Type | Human Otc Drug |
Proprietary Name | Lipotox |
Generic Name | Squalene, Cholesterinum, Estradiol, Progesterone, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methyl Paraben, Propyl Paraben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum, Arsenicum Album, Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Aceticum Acidum, Adrenocorticotrophin, Benzoicum Acidum, Benzyl Alcohol, Boricum Acidum, Chlorinum, Cortisone Aceticum, Eugenol, Folliculinum, Isopropyl Palmitate, Lacticum Acidum, Petroleum Jelly |
Dosage Form | Liquid |
Route of Administration | ORAL |
Marketing Start Date | 2016-01-11 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | BioActive Nutritional, Inc. |
Substance Name | SQUALENE; CHOLESTEROL; ESTRADIOL; PROGESTERONE; ASPARTAME; BENZALKONIUM CHLORIDE; FORMALDEHYDE; METHYLENE CHLORIDE; METHYLPARABEN; PROPYLPARABEN; SODIUM BENZOATE; ANHYDROUS TRISODIUM CITRATE; TITANIUM DIOXIDE; ZINC OXIDE; ARSENIC TRIOXIDE; LYCOPODIUM CLAVATUM SPORE; STRYCHNOS NUX-VOMICA SEED; PHOSPHORIC ACID; PHOSPHORUS; ACETIC ACID; CORTICOTROPIN; BENZOIC ACID; BENZYL ALCOHOL; BORIC ACID; CHLORINE; CORTISONE ACETATE; EUGENOL; ESTRONE; ISOPROPYL ALCOHOL; LACTIC ACID, DL-; PETROLATUM; PHENYLBUTAZONE; LEAD; POTASSIUM SORBATE; RESORCINOL; SALICYLIC ACID; SORBITOL; STEARYL ALCOHOL; XYLITOL |
Active Ingredient Strength | 8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2016-01-11 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-01-11 |
Ingredient | Strength |
---|---|
SQUALENE | 8 [hp_X]/mL |
NDC | Brand Name | Generic Name |
---|---|---|
43857-0143 | Lipotox | Squalene, Cholesterinum, Estrogen, Progesterone, Aspartame, Benzalkonium chloride, Formalinum, Methylene chloride |
43857-0384 | Lipotox | Squalene, Cholesterinum, Estradiol, Progesterone, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methyl Paraben, Propyl Paraben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum, Arsenicum Album, Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Aceticum Acidum, Adrenocorticotrophin, Benzoicum Acidum, Benzyl Alcohol, Boricum Acidum, Chlorinum, Cortisone Aceticum, Eugenol, Folliculinum, Isopropyl Palmitate, Lacticum Acidum, Petroleum Jelly |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() LIPOTOX 86665532 not registered Dead/Abandoned |
Jaffe, Andrew T. 2015-06-17 |
![]() LIPOTOX 86665532 not registered Dead/Abandoned |
Eshbaugh, Jr., Willis G. 2015-06-17 |
![]() LIPOTOX 78144461 not registered Dead/Abandoned |
Solux Corporation 2002-07-16 |